Category Archives: News, events, & announcements

2017-18 Abstract Competition Has Begun!

Call for Abstracts

Golden Helix strives to enable precision medicine by developing powerful software that supports researchers with complex analysis. One of my favorite events of the year is our abstract competition that expands on our mission. This competition allows us to support our community by recognizing innovative ways to conduct genomic analysis. I am pleased to announce that our 2017-18 Abstract Competition… Read more »

End of Year VarSeq Bundles

      Delaina Hawkins    November 28, 2017    No Comments on End of Year VarSeq Bundles

This week we’re featuring several VarSeq bundles that are part of our end of year pricing specials! VarSeq CNV PowerPack – $15,995 We’ve made tremendous progress integrating CNV analytics capabilities into VarSeq this year. The PowerPack bundle is a great solution for those who are interested in combining SNV and CNV analysis. SVS-VarSeq Bundle – $7,995 If you’re a researcher or… Read more »

Our End of Year Bundles Are Back!

In case you haven’t heard the big news … our end of year bundles are back by popular demand! There’s a little something for everyone so if you’ve had your eye on one of our products now is the time to buy! SVS Single-User License – $2,995 Wouldn’t it be great to be able to easily perform complex analyses and visualizations on… Read more »

Reflecting on ASHG 2017

      Andreas Scherer    October 26, 2017    No Comments on Reflecting on ASHG 2017
ASHG 2017

We’ve returned from another successful year at ASHG and had an incredible time. I find the conference to be a terrific opportunity to connect with our customers, partners, and friends in the industry. This year’s Presidential Symposium was a true delight featuring a discussion of global health and genomics between two absolute legends in the health and science world: Bill Gates,… Read more »

VarSeq Updated with CNV Annotations, CNV PhoRank and Region Assessment Catalogs

VarSeq Updated

VarSeq Updated with CNV Annotations, CNV PhoRank and Region Assessment Catalogs This year we have released multiple advances to support CNV analysis in VarSeq, expanding our target region based VS-CNV caller to handle exomes and low-depth genomes as well additional supporting algorithms like calling Loss of Heterozygosity regions. To top this off, VarSeq 1.4.7 has been shipped with many expanded… Read more »